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Related Concept Videos

Multi-species Conserved Sequences02:51

Multi-species Conserved Sequences

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Next-generation sequencing technologies have created large genomic databases of a variety of animals and plants. Ever since the human genome project was completed, scientists studied the genome of primates, mammals, and other phylogenetically distant living beings. Such large-scale  studies have provided new insights into the evolutionary relationship between organisms.
Although the genome of each species varies greatly from each other, a few sequences are highly conserved. Such conserved...
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Related Experiment Video

Updated: Apr 14, 2026

Identification of Key Factors Regulating Self-renewal and Differentiation in EML Hematopoietic Precursor Cells by RNA-sequencing Analysis
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A single workflow for multi-species blood transcriptomics.

Elody Orcel1, Hayat Hage1, May Taha1

  • 1BIOASTER, 40 Avenue Tony Garnier, Lyon, 69007, France.

BMC Genomics
|March 17, 2024
PubMed
Summary
This summary is machine-generated.

This study introduces a standardized RNA sequencing workflow for blood samples, enabling reliable multi-species transcriptomic analysis for vaccine and drug development. This improves inter-species comparisons and biomarker discovery.

Keywords:
Blood samplesClinical modelsData analysisLibrary preparationPreclinical modelsQuality controlsRNA extractionReportStandardizationTotal RNA sequencingTranscriptomicsWorkflow

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Area of Science:

  • Genomics
  • Immunology
  • Pharmacology

Background:

  • Blood transcriptomic analysis offers insights into physiological states and immune responses to vaccines.
  • Current multi-species transcriptomic analysis faces technological challenges and lacks standardized workflows for inter-species comparison.

Purpose of the Study:

  • To develop a single, comprehensive total RNA sequencing (RNA-Seq) workflow for generating reliable blood transcriptomic data from humans and preclinical animal models.
  • To establish standardized criteria and thresholds for validating transcriptomic workflows across species.

Main Methods:

  • A complete RNA-Seq workflow was applied to blood samples from humans, rabbits, non-human primates, and mice.
  • Workflow performance was rigorously evaluated using multiple wet-lab and dry-lab metrics.
  • An automated data analysis pipeline was developed to streamline dataset validation.

Main Results:

  • The proposed workflow successfully generated reliable transcriptomic data across four species.
  • Key validation criteria and thresholds were identified for assessing workflow performance.
  • Automated analysis facilitated efficient validation of generated transcriptomic datasets.

Conclusions:

  • An end-to-end workflow was developed to enhance standardization and inter-species comparison in blood transcriptomics.
  • This standardized approach allows direct comparison of preclinical and clinical RNA sequencing data for vaccine and drug development.
  • The workflow facilitates the identification of biomarkers for monitoring drug safety and vaccine efficacy.